Aperiodic electrophysiological activity in preterm infants is linked to subsequent autism risk. Issue 4 (20th April 2022)

• Record Type: Journal Article
• Authors: Shuffrey, Lauren C.; Pini, Nicolò; Potter, Mandy; Springer, Priscilla; Lucchini, Maristella; Rayport, Yael; Sania, Ayesha; Firestein, Morgan; Brink, Lucy; Isler, Joseph R.; Odendaal, Hein; Fifer, William P.
• Is Part Of: Developmental psychobiology. Volume 64:Issue 4(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-04-20
• Subjects: aperiodic EEG -- autism risk -- electroencephalography (EEG) -- infants -- neuronal oscillations -- preterm birth; Psychobiology -- Periodicals; 155
• DOI: 10.1002/dev.22271
• Languages: English
• ISSNs: 0012-1630

Abstract

Abstract: Approximately 7% of preterm infants receive an autism spectrum disorder (ASD) diagnosis. Yet, there is a significant gap in the literature in identifying prospective markers of neurodevelopmental risk in preterm infants. The present study examined two electroencephalography (EEG) parameters during infancy, absolute EEG power and aperiodic activity of the power spectral density (PSD) slope, in association with subsequent autism risk and cognitive ability in a diverse cohort of children born preterm in South Africa. Participants were 71 preterm infants born between 25 and 36 weeks gestation (34.60 ± 2.34 weeks). EEG was collected during sleep between 39 and 41 weeks postmenstrual age adjusted (40.00 ± 0.42 weeks). The Bayley Scales of Infant Development and Brief Infant Toddler Social Emotional Assessment (BITSEA) were administered at approximately 3 years of age adjusted (34 ± 2.7 months). Aperiodic activity, but not the rhythmic oscillatory activity, at multiple electrode sites was associated with subsequent increased autism risk on the BITSEA at three years of age. No associations were found between the PSD slope or absolute EEG power and cognitive development. Our findings highlight the need to examine potential markers of subsequent autism risk in high‐risk populations other than infants at familial risk.